Sechrist Industries, Inc.
4225 E LA PALMA AVE, Anaheim, CA, US
Registered product codes
8 product codes
Recent MDR events
537 on file
- SECHRIST INDUSTRIES INC.Jul 22, 2026Malfunction2020267-2026-00009
- SECHRIST INDUSTRIES INC.May 5, 2026Injury2020676-2026-00006
- SECHRIST INDUSTRIES INC.Apr 8, 2026Injury2020676-2026-00005
- SECHRIST INDUSTRIES INC.Mar 23, 2026Malfunction2020676-2026-00003
- SECHRIST INDUSTRIES INC.Jan 8, 2026Malfunction2020676-2026-00001
- SECHRIST INDUSTRIES INC.Nov 24, 2025Malfunction2020676-2025-00028
- STRYKERNov 21, 2025Injury2020676-2025-00029
- SECHRIST INDUSTRIES, INC.Oct 21, 2025Malfunction2020676-2025-00027
- SECHRIST INDUSTRIES, INC.Oct 21, 2025Malfunction2020676-2025-00026
- SECHRIST INDUSTRIES INC.Oct 20, 2025Malfunction2020676-2025-00025
Recalls
10 on file
- TerminatedJul 1, 2015
Sechrist Industries is recalling the Sechrist Low Profile Wheeled Stretcher because it may experience an unexpected incline angle during the height adjustment of the Low Profile Wheeled Stretcher when lifting the patient upward or when lowering the Wheeled Stretcher to a height at which the patient can be loaded/unloaded.
View FDA record ↗ - TerminatedNov 6, 2012
Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with Electronic Control Modules in order to correct a software bug that could potentially affect the performance of the chamber.
View FDA record ↗ - TerminatedNov 6, 2012
Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with Electronic Control Modules in order to correct a software bug that could potentially affect the performance of the chamber.
View FDA record ↗ - TerminatedJan 19, 2012
Stryker Medical has received complaints from customers that indicate a bushing in the braking system may fracture, which could result in the brake/steer pedal seizing. If the pedal seizes, the braking system may become inoperable or steering around corners may come more difficult. While no injuries have been associated with these reported events nor has there been reported failure events resulting
View FDA record ↗ - TerminatedJan 18, 2008
Brake Problems: The stretcher brake cams may crack while attempting to lock the stretcher brake (Sechrist is supplied the stretchers by the manufacturer Stryker Medical)
View FDA record ↗ - TerminatedJan 18, 2008
Brake Problems: The stretcher brake cams may crack while attempting to lock the stretcher brake (Sechrist is supplied the stretchers by the manufacturer Stryker Medical)
View FDA record ↗ - TerminatedJan 18, 2008
Brake Problems: The stretcher brake cams may crack while attempting to lock the stretcher brake (Sechrist is supplied the stretchers by the manufacturer Stryker Medical)
View FDA record ↗ - TerminatedJan 18, 2008
Brake Problems: The stretcher brake cams may crack while attempting to lock the stretcher brake (Sechrist is supplied the stretchers by the manufacturer Stryker Medical)
View FDA record ↗ - TerminatedJan 18, 2008
Brake Problems: The stretcher brake cams may crack while attempting to lock the stretcher brake (Sechrist is supplied the stretchers by the manufacturer Stryker Medical)
View FDA record ↗ - TerminatedJul 20, 2004
Electronic manometer malfunctions. Manometer may be illegible. The alarm for power failure may function only briefly, or not at all.
View FDA record ↗
Compliance history
Matched by FEI 2020676.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.